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Forwarded from Let's Grow Upper Egypt (Yussof Wahba)
#QC #QA #Validation_Section_Head #QA_Manager

Sigma Group for pharmaceutical industries believes that Successful people are the company׳s most important asset.
We are seeking for:
Quality Assurance Manager (Ref: QAM)
Validation Section Head (Ref: V S C)
Quality Assurance Specialist (Ref: QAS)
Quality Control Specialist (Ref: QCS)

With the following requirements:

For (Ref: QAS) The Right candidate should be:
•Delta Resident.
•BScs. of Pharmacy.
•Experience is a must.
•Managerial and leadership capabilities.
•Analytical thinking.
•Excellent communication skills.
•Fluent in English. both in writing and speech.

For (Ref: VSC) & (Ref: QAS) & (QCS) The Right candidate should be
• Delta Resident.
• BScs. of science,
Experience is a must for (Ref: VSC).
Experience or fresh graduate for (Ref: QAS) & (QCS).
• Analytical thinking.
•Excellent communication skills.
•Fluent in English. both in writing and speech.


If you find yourself suitable for the requested position, kindly send your updated CV with recent photo to e-mail:
Careers@sigma-pharm.com
Please, Mention the requested position (Ref) in email subject.
Good luck..
Egypt Otsuka is hiring now:

Validation & Calibration Supervisor

Main Duties :

Create , execute and Revise of the validation lifecycle documentation for the :
- Equipment qualification and CSV,
- HVAC and area qualification activities within the facility
- Thermal mapping activity
- Aseptic Process simulation 
- Utility Qualification

-Plan, perform and document validation activities in conjunction with Validation Team and area heads. 
- Author, execution, Participate in Designs in the of validation protocols.
-Ensure integration of Risk based approach for designing the qualification and validation activities 
-Ensure validation studies of the operations and quality control facilities, the utilities serving the facilities and manufacturing/operations areas, and testing equipment are completed to the required cGMP standards.
- Maintain the Revalidation Plan for the manufacturing and quality control facilities, the utilities serving the facilities , and manufacturing equipment 
- Create /Review/audit key validation deliverables and change control deliverables.
- Ensure that GMP standards are applied based on Local Authority, WHO requirements and Otsuka standards.

Qualifications :

- Bch. In Engineering, Pharmacy or Science 
- Minimum of 6 years of experience in the field. 
- Excellent English, verbal / written communication
- Excellent computer skills
- High Analytical thinking & Problem solving 
- Management, leadership and decision making skills

- Work Location : 10th of Ramadan
for the interested candidates please send your cv to
marwa.safa@egyptotsuka.com


https://www.linkedin.com/posts/marwa-safa-01617a90_validation-engineering-pharmacy-activity-7221860301078425600-puMn?utm_source=share&utm_medium=member_android
#QA_Validation_Specialist_Vacancy #validation
Quality Assurance Validation Specialist Vacancy

U-Pharma is a market leader pharmaceutical manufacturing Company, located in 10th of Ramadan City, is hiring for Quality Assurance Validation specialist in the Quality Assurance Department
Requirements:
0-2 years of experience, preferably in sterile manufacturing, Fresh graduates are also encouraged to apply
·Residency in 10th of Ramadan city , AL Tagamoa ,Zagazig , Al-Obour City , Al-Shrouk city or Nasr city, Banha, Kafr Shukr, Deyarb Negm
Interested candidates are kindly requested to send their updated CVs with recent photo to Recruitment@upharmaegypt.com and mention the job code in the subject field.


https://www.linkedin.com/posts/u-pharma-careers_vacancy-qaabrvalidationabrspecialistabrvacancy-activity-7234476087643111425-tUQD?utm_source=share&utm_medium=member_android
Egypt Otsuka is hiring now:

Validation & Calibration Supervisor

Main Duties :

Create , execute and Revise of the validation lifecycle documentation for the :
- Equipment qualification and CSV,
- HVAC and area qualification activities within the facility
- Thermal mapping activity
- Aseptic Process simulation
- Utility Qualification

-Plan, perform and document validation activities in conjunction with Validation Team and area heads.
- Author, execution, Participate in Designs in the of validation protocols.
-Ensure integration of Risk based approach for designing the qualification and validation activities
-Ensure validation studies of the operations and quality control facilities, the utilities serving the facilities and manufacturing/operations areas, and testing equipment are completed to the required cGMP standards.
- Maintain the Revalidation Plan for the manufacturing and quality control facilities, the utilities serving the facilities , and manufacturing equipment
- Create /Review/audit key validation deliverables and change control deliverables.
- Ensure that GMP standards are applied based on Local Authority, WHO requirements and Otsuka standards.

Qualifications :

- Bch. In Engineering, Pharmacy or Science
- Minimum of 6 years of experience in the field.
- Excellent English, verbal / written communication
- Excellent computer skills
- High Analytical thinking & Problem solving
- Management, leadership and decision making skills

- Work Location : 10th of Ramadan
for the interested candidates please send your cv to
marwa.safa@egyptotsuka.com


https://www.linkedin.com/posts/marwa-safa-01617a90_validation-engineering-pharmacy-activity-7243920697255772161-8JtT?utm_source=share&utm_medium=member_android
👍1
TAB Egypt is hiring Validation Specialist with the below qualifications:-

Bachelor's degree in Engineering or Science.
Solid experience at least 2-5 years in pharmaceutical validation activities.
Knowledge of regulatory requirements and industry standards (GMP, ISO 14644, WHO etc.)
Basic Knowledge of HVAC Testing, Thermal Mapping studies.
Excel is a must

Kindly send your CV to HR@tab.com.eg with the subject “Validation Specialist”.

https://www.linkedin.com/posts/menna-mohamed-17081119a_validation-validationjobs-pharmaceutical-activity-7282754897563803648-I0Nj?utm_source=share&utm_medium=member_android
🚀 Exciting Career Opportunities at MEVAC – Join Our Quality Team! 🚀

Are you passionate about quality control, quality assurance, and validation in the animal vaccine industry? 
MEVAC is expanding its Quality team and looking for talented professionals to join us!

Here’s a quick look at our open roles:

1️⃣ Computerized System Validation (CSV) Specialist – QA
🔹 Bachelor’s in Science/Computer Science
🔹 1+ years in CSV (pharma/biotech)
🔹 Knowledge of FDA 21 CFR Part 11, GAMP 5, EU Annex 11
🔹 Experience in validation protocols (IQ/OQ/PQ), risk assessments, and compliance

2️⃣ Validation Specialist – QA
🔹 Experience in pharma/vaccine manufacturing validation
🔹 Strong understanding of GMP and regulatory standards

3️⃣ QC Documentation Specialist
🔹 Excellent English skills (writing & documentation)
🔹 No specific degree required – open to all backgrounds!

4️⃣ QC Specialist (Fresh Graduates Welcome!)
🔹 Veterinary degree holders preferred
🔹 No experience needed – training provided!

5️⃣ QC Specialist (Chemical Background)
🔹 Strong knowledge in chemical testing & analysis
🔹 Relevant educational background


📍Location : Salhya El-Gedida (Sharkia)


Why MEVAC? 💡
Impact Lives: Help create vaccines that protect animals worldwide.
Grow with Us: Professional development and innovation are at our core.
Cutting-Edge Tech: Work with the latest tools in animal vaccine manufacturing.

📩 Interested? Send your CV to jobs@me-vac.com or tag someone who’d be a great fit!
(Don't forget to mention the title in the subject)

Let’s shape the future of animal health together! 🌍🐾

#Hiring #QualityControl #QualityAssurance #Vaccines #CSV #Validation #MevacCareers #NowHiring #JoinOurTeam

https://www.linkedin.com/posts/nadamaher97_hiring-qualitycontrol-qualityassurance-activity-7318650796860956672-3q0X?utm_source=share&utm_medium=member_android&rcm=ACoAAEmhAc0BR4cUJKYw7VVgS9xtWl-oUXC_I34
#Orchidia #pharmaceutical located in Oubor is hiring the below #positions:

1- #planning specialist :
(pharmacist / chemist- minimum experience 1 to 3 years)

2- #toll planning specialist / senior :
(pharmacist / chemist - 1 to 5 years in toll manufacturing)

3- #logistics specialist :
( Bachelor's degree in logistics- minimum 1 year of exp in logistics)

4- #Production Pharmacist :
(pharmacist - minimum 1 year of exp in sterile area)

5- R&D #Formulation / specialist :
(Pharmacist- minimum 1 year of exp in formulation)

6- R&D #Validation & #Methodology Analyst :
(Pharmacist/ Chemist- minimum 1 years of exp in Validation and Methodology analysis)

Interested Candidates send their CVs to ahmed.elghamrawy@orchidiapharmaceutical.com Mentioning position name in subject .


https://www.linkedin.com/posts/ahmed-elghamarawy-8a0325105_orchidia-pharmaceutical-positions-activity-7322563224107687937-SVXn?utm_source=share&utm_medium=member_android&rcm=ACoAAEmhAc0BR4cUJKYw7VVgS9xtWl-oUXC_I34
👍1
TAB Egypt is hiring Validation Specialist with the below qualifications:-

Bachelor's degree in Engineering or Science.
Solid experience at least 2-5 years in pharmaceutical validation activities.
Knowledge of regulatory requirements and industry standards (GMP, ISO 14644, WHO etc.)
Basic Knowledge of HVAC Testing, Thermal Mapping studies.
Excel is a must

Kindly send your CV to HR@tab.com.eg with the subject “Validation Specialist”.


https://www.linkedin.com/posts/menna-mohamed-17081119a_validation-validationjobs-pharmaceutical-activity-7330136236474449920-z2T9?utm_source=share&utm_medium=member_android&rcm=ACoAAEmhAc0BR4cUJKYw7VVgS9xtWl-oUXC_I34
👍1
#Orchidia #pharmaceutical located in Oubor is hiring the below
#positions:

1- #Warehouse #Manager :
( Pharmacist / Chemist - 10 to 15 years in Warehouses Pharmaceutical Manufacturing )

2- #Foreign #purchasing Specialist
(Pharmacist/ Chemist- minimum 2 years of exp in foreign purchasing)

3- #QA #Documentation Section head :
( Pharmacist / Chemist - minimum 7 years of exp in Documentation )

4- #QA #Validation Specialist :
(Pharmacist / chemist - minimum 2 years of exp in validation )

5- #QC #finished product Analyst/ Senior :
(Pharmacist - minimum 1 year of exp in QC finished product analysis)

Interested Candidates send their CVs to ahmed.elghamrawy@orchidiapharmaceutical.com Mentioning position name in subject


https://www.linkedin.com/posts/ahmed-elghamarawy-8a0325105_orchidia-pharmaceutical-positions-activity-7333119903526191104-VUWY?utm_source=share&utm_medium=member_android&rcm=ACoAAEmhAc0BR4cUJKYw7VVgS9xtWl-oUXC_I34
#Orchidia #pharmaceutical located in Oubor is hiring the below
#positions:

1- #Warehouse #Manager :
( Pharmacist / Chemist - 10 to 15 years in exp Warehouses Pharmaceutical Manufacturing )

2- #Foreign #purchasing Specialist
(Pharmacist/ Chemist- minimum 2 years of exp in foreign purchasing)

3- #QA Section head :
(pharmacist minimum 8 years in validation & IPC & Compliance)

4- #QA #Documentation Section head :
( Pharmacist / Chemist - minimum 8 years of exp in Documentation )

5- #QA #Validation Specialist :
(Pharmacist / chemist - minimum 2 years of exp in validation )

6- #QC #finished product Analyst/ Senior :
(Pharmacist - minimum 1 year of exp in QC finished product analysis)

7- #microbiologist / Senior microbiologist :
(Pharmacist / Chemist minimum 1 to 5 years exp in micro)

Interested Candidates send their CVs to ahmed.elghamrawy@orchidiapharmaceutical.com Mentioning position name in subject

https://www.linkedin.com/posts/ahmed-elghamarawy-8a0325105_orchidia-pharmaceutical-positions-activity-7338193906854981637-MhRb?utm_source=share&utm_medium=member_android&rcm=ACoAAEmhAc0BR4cUJKYw7VVgS9xtWl-oUXC_I34
1
#Validation Specialist – #Sterile Pharmaceutical Manufacturing
Key Responsibilities:
Assist in preparing and executing calibration & Qualification plans.
Assist in preparing and executing validation protocols (IQ/OQ/PQ)
Support aseptic process simulations (media fills), cleaning validation, and documentation
Work closely with QA, Engineering, and Production teams

Qualifications:
Bachelor’s degree in Pharmacy or Science.
Familiarity with GMP and sterile manufacturing (internships/projects a plus)
Strong attention to detail and willingness to learn.
Experience from 0:2 year
interested candidates send CVs to : eali@sunnyph.com , mentioned the job title in the subject line.


https://www.linkedin.com/posts/sunny-pharmaceutical_validation-sterile-activity-7359165514079776771-gJCW?utm_source=share&utm_medium=member_android&rcm=ACoAAEmhAc0BR4cUJKYw7VVgS9xtWl-oUXC_I34
#Validation Specialist – #Sterile Pharmaceutical Manufacturing
Key Responsibilities:
Assist in preparing and executing calibration & Qualification plans.
Assist in preparing and executing validation protocols (IQ/OQ/PQ)
Support aseptic process simulations (media fills), cleaning validation, and documentation
Work closely with QA, Engineering, and Production teams

Qualifications:
Bachelor’s degree in Pharmacy or Science.
Familiarity with GMP and sterile manufacturing (internships/projects a plus)
Strong attention to detail and willingness to learn.
Experience from 0:2 year

interested candidates send CVs to :
eali@sunnyph.com

, mentioned the job title in the subject line


https://www.linkedin.com/posts/esraa-ali-1581a36a_validation-sterile-activity-7363532908361302018-RQHx?utm_source=share&utm_medium=member_android&rcm=ACoAAEmhAc0BR4cUJKYw7VVgS9xtWl-oUXC_I34